ProductGuru Recalls

Official recall record

Alcon Ophthalmic Knife

Health Canada — Medical Devices · 2024-05-08 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2024-05-08
Last updated (per notice)
2024-08-18
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

On April 24, 2024 Alcon Canada was notified of an increase in customer reports of dull or knife not sharp for specific ClearCut® Dual Bevel Sideport and A-OK® Corneal/Scleral V-lance ophthalmic knives. Knives that do not meet customer sharpness expectations could result in the use of increased penetration force during surgery when compared to a sharper knife. The initial scope was based on an observed in-process data shift for a specific knife family. Based on the new complaint signal, out of an abundance of caution, Alcon is now including all blades, of all models, made August 1, 2023 to March 2, 2024. Recall start date: April 26, 2024

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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